Síntese e avaliação de novos análogos aril-acilidrazônicos do canabidiol

Detalhes bibliográficos
Ano de defesa: 2019
Autor(a) principal: Franco, Graziella Dos Reis Rosa lattes
Orientador(a): Viegas Júnior, Cláudio lattes
Banca de defesa: Lopardi, Lucas, Ceron, Carla Speroni
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Alfenas
Programa de Pós-Graduação: Programa de Pós-Graduação em Química
Departamento: Instituto de Ciências Exatas
País: Brasil
Palavras-chave em Português:
Área do conhecimento CNPq:
Link de acesso: https://repositorio.unifal-mg.edu.br/handle/123456789/1338
Resumo: This work focused on the synthesis of rationally drug designed, inspired by the structure of canabidiol (CBD), with R and S-carvone as starting materials. Eight substances named PQM-242 to PQM-249, with novel structural pattern, were synthesized, characterized and evaluated by in silico and pharmacological models. The analysis of the scavenging activity of DPPH radicals showed their antioxidant properties similar to quercetin and ascorbic acid, especially for PQM-247 with IC50 of 4.76μM and a good metal chelating activity, especially for Zn2+. The in silico study suggested that PQM-244, PQM-245, PQM-248 and PQM-249 have adequate ability for overcoming the blood brain barrier, leading to better CNS activity, whereas molecular docking studies showed that the target-compounds have good affinities for cannabinoid receptors, especially for CB1, for which PQM-249 exhibited an affinity slightly greater than CBD. In vitro pharmacological evaluation showed that the target-substances are not cytotoxic, except for PQM-244 and PQM-247, which exhibited CC50 values of 2.92 and 7.95 μM, respectively. In the antidepressive-type models (forced swimming test and tail suspension test) and anxiolytic-type models (open field test and light-dark test), the substances did not show an anxiolytic effect. However, they have been shown to act as antidepressants in the dose of 100μM (10mg/kg for CBD), highlighting compound PQM-249 that showed antidepressant effect in both tests.
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spelling Franco, Graziella Dos Reis Rosahttp://lattes.cnpq.br/1381066386437549Gontijo, Vanessa SilvaLopardi, LucasCeron, Carla SperoniViegas Júnior, Cláudiohttp://lattes.cnpq.br/75339230997893612019-04-03T21:09:05Z2019-02-08FRANCO, Graziella dos Reis Rosa. Síntese e avaliação de novos análogos aril-acilidrazônicos do canabidiol. 2019. 139 f. Dissertação (Mestrado em Química) - Universidade Federal de Alfenas, Alfenas, MG, 2019.https://repositorio.unifal-mg.edu.br/handle/123456789/1338This work focused on the synthesis of rationally drug designed, inspired by the structure of canabidiol (CBD), with R and S-carvone as starting materials. Eight substances named PQM-242 to PQM-249, with novel structural pattern, were synthesized, characterized and evaluated by in silico and pharmacological models. The analysis of the scavenging activity of DPPH radicals showed their antioxidant properties similar to quercetin and ascorbic acid, especially for PQM-247 with IC50 of 4.76μM and a good metal chelating activity, especially for Zn2+. The in silico study suggested that PQM-244, PQM-245, PQM-248 and PQM-249 have adequate ability for overcoming the blood brain barrier, leading to better CNS activity, whereas molecular docking studies showed that the target-compounds have good affinities for cannabinoid receptors, especially for CB1, for which PQM-249 exhibited an affinity slightly greater than CBD. In vitro pharmacological evaluation showed that the target-substances are not cytotoxic, except for PQM-244 and PQM-247, which exhibited CC50 values of 2.92 and 7.95 μM, respectively. In the antidepressive-type models (forced swimming test and tail suspension test) and anxiolytic-type models (open field test and light-dark test), the substances did not show an anxiolytic effect. However, they have been shown to act as antidepressants in the dose of 100μM (10mg/kg for CBD), highlighting compound PQM-249 that showed antidepressant effect in both tests.Este trabalho teve seu enfoque na síntese de análogos racionalmente planejados, inspirados na estrutura do canabidiol (CBD), tendo as R- e S-carvonas como materiais de partida. Foram sintetizadas, caracterizadas e avaliadas por estudos in silico e farmacológicos 8 substâncias denominadas PQM-242 a PQM-249 com padrão estrutural inédito. A análise da atividade sequestrante de radicais DPPH mostrou que as substâncias apresentaram propriedades antioxidantes semelhantes à quercetina e ao ácido ascórbico, com destaque para PQM-247, com CI50= 4,76μM e um bom perfil quelante de metais, especialmente para Zn2+. O estudo in silico das propriedades ADME sugeriu que PQM-244, PQM-245, PQM-248 e PQM-249 têm a possibilidade de ultrapassar a barreira hematoencefálica, gerando uma melhor atividade no SNC, enquanto que o docking molecular mostrou que os compostos-alvo possuem uma boa afinidade com os receptores canabinoides, especialmente com o receptor CB1, para o qual a PQM-249 exibiu uma afinidade discretamente maior que o CBD. A avaliação farmacológica in vitro mostrou que as substâncias não são citotóxicas, à exceção de PQM-244 e PQM-247 que apresentaram valores de CC50 de 2,92 e 7,95μM, respectivamente. Nos modelos de atividade tipo-antidepressiva (teste de nado forçado e teste de suspensão pela cauda) e tipo-ansiolítica (teste de campo aberto e teste claro-escuro), as substâncias não demonstraram efeito ansiolítico. Entretanto, os resultados indicaram que elas atuam como antidepressivos na dose de 100μM (10mg/Kg para o CBD) com destaque para PQM-249 que mostrou efeito antidepressivo em ambos os ensaios.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESapplication/pdfporUniversidade Federal de AlfenasPrograma de Pós-Graduação em QuímicaUNIFAL-MGBrasilInstituto de Ciências Exatasinfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-nd/4.0/CanabidiolCanabinoidesDoenças NeurodegenerativasAntioxidantesAntidepressivosQUIMICA::QUIMICA ORGANICASíntese e avaliação de novos análogos aril-acilidrazônicos do canabidiolinfo:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/publishedVersion-8156311678363143599600600600-81940697172828021542075167498588264571reponame:Repositório Institucional da Universidade Federal de Alfenas - RiUnifalinstname:Universidade Federal de Alfenas (UNIFAL)instacron:UNIFALFranco, Graziella Dos Reis RosaLICENSElicense.txtlicense.txttext/plain; charset=utf-81987https://repositorio.unifal-mg.edu.br/bitstreams/ff6b8076-749e-4446-92be-0d4af9aaa1cb/download31555718c4fc75849dd08f27935d4f6bMD51CC-LICENSElicense_urllicense_urltext/plain; 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dc.title.pt-BR.fl_str_mv Síntese e avaliação de novos análogos aril-acilidrazônicos do canabidiol
title Síntese e avaliação de novos análogos aril-acilidrazônicos do canabidiol
spellingShingle Síntese e avaliação de novos análogos aril-acilidrazônicos do canabidiol
Franco, Graziella Dos Reis Rosa
Canabidiol
Canabinoides
Doenças Neurodegenerativas
Antioxidantes
Antidepressivos
QUIMICA::QUIMICA ORGANICA
title_short Síntese e avaliação de novos análogos aril-acilidrazônicos do canabidiol
title_full Síntese e avaliação de novos análogos aril-acilidrazônicos do canabidiol
title_fullStr Síntese e avaliação de novos análogos aril-acilidrazônicos do canabidiol
title_full_unstemmed Síntese e avaliação de novos análogos aril-acilidrazônicos do canabidiol
title_sort Síntese e avaliação de novos análogos aril-acilidrazônicos do canabidiol
author Franco, Graziella Dos Reis Rosa
author_facet Franco, Graziella Dos Reis Rosa
author_role author
dc.contributor.author.fl_str_mv Franco, Graziella Dos Reis Rosa
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/1381066386437549
dc.contributor.advisor-co1.fl_str_mv Gontijo, Vanessa Silva
dc.contributor.referee1.fl_str_mv Lopardi, Lucas
dc.contributor.referee2.fl_str_mv Ceron, Carla Speroni
dc.contributor.advisor1.fl_str_mv Viegas Júnior, Cláudio
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/7533923099789361
contributor_str_mv Gontijo, Vanessa Silva
Lopardi, Lucas
Ceron, Carla Speroni
Viegas Júnior, Cláudio
dc.subject.por.fl_str_mv Canabidiol
Canabinoides
Doenças Neurodegenerativas
Antioxidantes
Antidepressivos
topic Canabidiol
Canabinoides
Doenças Neurodegenerativas
Antioxidantes
Antidepressivos
QUIMICA::QUIMICA ORGANICA
dc.subject.cnpq.fl_str_mv QUIMICA::QUIMICA ORGANICA
description This work focused on the synthesis of rationally drug designed, inspired by the structure of canabidiol (CBD), with R and S-carvone as starting materials. Eight substances named PQM-242 to PQM-249, with novel structural pattern, were synthesized, characterized and evaluated by in silico and pharmacological models. The analysis of the scavenging activity of DPPH radicals showed their antioxidant properties similar to quercetin and ascorbic acid, especially for PQM-247 with IC50 of 4.76μM and a good metal chelating activity, especially for Zn2+. The in silico study suggested that PQM-244, PQM-245, PQM-248 and PQM-249 have adequate ability for overcoming the blood brain barrier, leading to better CNS activity, whereas molecular docking studies showed that the target-compounds have good affinities for cannabinoid receptors, especially for CB1, for which PQM-249 exhibited an affinity slightly greater than CBD. In vitro pharmacological evaluation showed that the target-substances are not cytotoxic, except for PQM-244 and PQM-247, which exhibited CC50 values of 2.92 and 7.95 μM, respectively. In the antidepressive-type models (forced swimming test and tail suspension test) and anxiolytic-type models (open field test and light-dark test), the substances did not show an anxiolytic effect. However, they have been shown to act as antidepressants in the dose of 100μM (10mg/kg for CBD), highlighting compound PQM-249 that showed antidepressant effect in both tests.
publishDate 2019
dc.date.accessioned.fl_str_mv 2019-04-03T21:09:05Z
dc.date.issued.fl_str_mv 2019-02-08
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
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dc.identifier.citation.fl_str_mv FRANCO, Graziella dos Reis Rosa. Síntese e avaliação de novos análogos aril-acilidrazônicos do canabidiol. 2019. 139 f. Dissertação (Mestrado em Química) - Universidade Federal de Alfenas, Alfenas, MG, 2019.
dc.identifier.uri.fl_str_mv https://repositorio.unifal-mg.edu.br/handle/123456789/1338
identifier_str_mv FRANCO, Graziella dos Reis Rosa. Síntese e avaliação de novos análogos aril-acilidrazônicos do canabidiol. 2019. 139 f. Dissertação (Mestrado em Química) - Universidade Federal de Alfenas, Alfenas, MG, 2019.
url https://repositorio.unifal-mg.edu.br/handle/123456789/1338
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dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv Instituto de Ciências Exatas
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